ConductScience.org, home

Trial · NCT07877207

AI-Supported CBT-Based Psychoeducation for Caregivers of Individuals With Schizophrenia

NCT07877207, Not applicable, Not yet recruiting, Kastamonu University

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. AI-Supported CBT-Based Psychoeducation for Caregivers of Individuals With Schizophrenia. Trials, record NCT07877207. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07877207

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
AI-Supported CBT-Based Psychoeducation for Caregivers of Individuals With Schizophrenia
NCT number
NCT07877207
Status
Not yet recruiting
Phases
Not applicable
Enrollment
88 participants, estimated
Lead sponsor
Kastamonu University
Conditions
Schizophrenia Caregiver, Caregiver Burden, Emotional Expressivity
Interventions
Control, Interactive AI-Supported Learning Activities, AI-Supported Cognitive Behavioral Approach-Based Psychoeducation Program
First posted
2026-10-16
Last updated
2026-10-16

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in Emotional Expressivity Assessed by the Emotional Expressivity ScaleBaseline (T0) and immediately after the six-week intervention (T1)
Emotional expressivity will be assessed using the Turkish version of the Emotional Expressivity Scale (EES). The scale consists of 15 items rated on a 7-point scale and includes three subscales: expression of intimacy, expression of positive emotions, and expression of negative emotions. Items 6 and 14 are reverse-scored. The total score ranges from 15 to 105, with higher scores indicating a greater tendency to express emotions. The outcome will be the change in the total and subscale scores from baseline to immediately after the six-week intervention. Changes over time will be compared between the intervention and control groups.
PrimaryChange in Caregiver Burden Assessed by the Zarit Burden InterviewBaseline (T0) and immediately after the six-week intervention (T1)
Caregiver burden will be assessed using the Zarit Burden Interview (ZBI), developed by Zarit, Reever, and Bach-Peterson (1980) and adapted into Turkish by İnci and Erdem (2008). The scale consists of 22 items rated from 0 (never) to 4 (nearly always). The total score ranges from 0 to 88, with higher scores indicating greater caregiver burden. The change in total score from baseline to post-intervention will be compared between the intervention and control groups.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07877207

GET https://conductscience.org/api/trials/v1/NCT07877207/registered